Guanosine stimulates neurite outgrowth in PC12 cells via activation of heme oxygenase and cyclic GMP

被引：45

作者：

Bau C. ^{[1
]}

Middlemiss P.J. ^{[1
]}

Hindley S. ^{[1
]}

Jiang S. ^{[1
]}

Ciccarelli R. ^{[2
]}

Caciagli F. ^{[2
]}

DiIorio P. ^{[2
]}

Werstiuk E.S. ^{[1
]}

Rathbone M.P. ^{[1
]}

机构：

[1] Department of Medicine, McMaster University, Health Sciences Centre, Hamilton, Ont.

[2] Department of Biomedical Sciences, School of Medicine, University of Chiete, Chieti

来源：

Purinergic Signalling | 2005年 / 1卷 / 2期

关键词：

Carbon monoxide; Cyclic GMP; Guanosine; Heme oxygenase; Neurite outgrowth; NGF; Nitric oxide synthase; PC12; cells;

D O I：

10.1007/s11302-005-6214-0

中图分类号：

学科分类号：

摘要：

Undifferentiated rat pheochromocytoma (PC12) cells extend neurites when cultured in the presence of nerve growth factor (NGF). Extracellular guanosine synergistically enhances NGF-dependent neurite outgrowth. We investigated the mechanism by which guanosine enhances NGF-dependent neurite outgrowth. Guanosine administration to PC12 cells significantly increased guanosine 3′,5′-cyclic monophosphate (cGMP) within the first 24 h whereas addition of soluble guanylate cyclase (sGC) inhibitors abolished guanosine-induced enhancement of NGF-dependent neurite outgrowth. sGC may be activated either by nitric oxide (NO) or by carbon monoxide (CO). Nw-Nitoro-L-arginine methyl ester (L-NAME), a non-isozyme selective inhibitor of nitric oxide synthase (NOS), had no effect on neurite outgrowth induced by guanosine. Neither nNOS (the constitutive isoform), nor iNOS (the inducible isoform) were expressed in undifferentiated PC12 cells, or under these treatment conditions. These data imply that NO does not mediate the neuritogenic effect of guanosine. Zinc protoporphyrin-IX, an inhibitor of heme oxygenase (HO), reduced guanosine-dependent neurite outgrowth but did not attenuate the effect of NGF. The addition of guanosine plus NGF significantly increased the expression of HO-1, the inducible isozyme of HO, after 12 h. These data demonstrate that guanosine enhances NGF-dependent neurite outgrowth by first activating the constitutive isozyme HO-2, and then by inducing the expression of HO-1, the enzymes responsible for CO synthesis, thus stimulating sGC and increasing intracellular cGMP. © Springer 2005.

引用

页码：161 / 172

页数：11

共 86 条

[41]

Kitamura Y., Matsuoka Y., Nomura Y., Taniguchi T., Induction of inducible nitric oxide synthase and heme oxygenase-1 in rat glial cells, Life Sci., 62, pp. 1717-1721, (1998)

[42]

Polte T., Oberle S., Schroder H., The nitric oxide donor SIN-1 protects endothelial cells from tumor necrosis factor-α mediated cytotoxicity: Possible role for cyclic GMP and heme oxygenase, J. Mol. Cell Cardiol., 29, pp. 3305-3310, (1997)

[43]

Demple B., Signal transduction by nitric oxide in cellular stress responses, Mol. Cell Biochem., 234-235, pp. 11-18, (2002)

[44]

Gunning P.W., Landreth G.E., Bothwell M.A., Shooter E.M., Differential and synergistic actions of nerve growth factor and cyclic AMP in PC12 cells, J. Cell Biol., 89, pp. 240-245, (1981)

[45]

Whalin M.E., Scammell J.G., Strada S.J., Thompson W.J., Phosphodiesterase II, the cGMP-activatable cyclic nucleotide phosphodiesterase, regulates cyclic AMP metabolism in PC12 cells, Mol. Pharmacol., 39, pp. 711-717, (1991)

[46]

Martin W., Villani G.M., Jothianandan D., Furchgott R.F., Selective blockade of endothelium-dependent and glyceryl trinitrate-induced relaxation by hemoglobin and by methylene blue in the rabbit aorta, J. Pharmacol. Exp. Ther., 232, pp. 708-716, (1985)

[47]

Mayer B., Brunner F., Schmidt K., Inhibition of nitric oxide synthesis by methylene blue, Biochem. Pharmacol., 45, pp. 367-374, (1993)

[48]

O'Donnell M.E., Owen N.E., Role of cyclic GMP in atrial natriuretic factor stimulation of Na+, K+, Cl- cotransport in vascular smooth muscle cells, J. Biol. Chem., 261, pp. 15461-15466, (1986)

[49]

Schmidt H.H., Endogenous soluble guanylyl cyclase-activating factors, FEBS Lett., 307, pp. 102-107, (1992)

[50]

Bogle R.G., Moncada S., Pearson J.D., Mann G.E., Identification of inhibitors of nitric oxide synthase that do not interact with the endothelial cell L-arginine transporter, Br. J. Pharmacol., 105, pp. 768-770, (1992)

← 1 2 3 4 5 6 7 8 9 →